- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06386055
Air Pollution and Physical Activity Study (PARC)
Air Pollution and Physical Activity
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a pilot randomized, control, clinical trial.
We will recruit 24 adults in Buffalo and randomize them to the physical intervention groups. The intervention group will be provided with physical activity courses.
We will follow up all participants until the end of the study.
We will collect their baseline information via questionnaire, and at the end of the follow-up we will collect the exit questionnaire and biospecimen.
The study aims to demonstrate our ability to recruit eligible participants and provide data of the compliance of participants to the intervention.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
Buffalo, New York, United States, 14214
- University at Buffalo
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- age 35-55 years old
- plan to stay in Buffalo most of the time in the next three months
- no adverse conditions
Exclusion Criteria:
• those with unstable or life-threatening medical conditions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group 1
This is the physical intervention group 1(n=8).
|
The intervention group will be provided with training courses for 3 months.
|
|
Experimental: Intervention group 2
This is the physical intervention group 2(n=8).
|
The intervention group will be provided with training courses for 3 months.
|
|
No Intervention: Control group
This is the control group (n=8).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
blood pressure
Time Frame: 3 months
|
blood pressure will be measured
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-report questionnaire
Time Frame: 3 months
|
This includes how participants feel about the intervention program
|
3 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Lina Mu, MD,PhD, State University of New York at Buffalo
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Behavior
- Sedentary Behavior
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Therapeutics
- Physical Therapy Modalities
- Patient Care
- Exercise Therapy
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Exercise
- Muscle Stretching Exercises
Other Study ID Numbers
- STUDY00007545
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.